Effects of cerivastatin and parathyroid hormone on the lumbar vertebra of aging male Sprague-Dawley rats

被引:14
作者
Banu, J [1 ]
Kalu, DN [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Physiol, San Antonio, TX 78229 USA
关键词
male Sprague-Dawley (SD) rats; cerivastatin; parathyroid hormone (PTH); lumbar vertebra;
D O I
10.1016/S8756-3282(02)00803-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Both men and women lose bone at a late age (aging bone loss). The aim of this study was to determine whether cerivastatin and parathyroid hormone (PTH) can prevent aging bone loss in men. Bone loss in aged male Sprague-Dawley (SD) rats was used as a model for age-related bone loss in men. Nine-month-old male SD rats were divided into six groups: (1) baseline controls (killed at the beginning of the study); (2) age-matched controls; (3) parathyroid hormone (PTH; 80 mug/kg body weight per day for 5 days/week) treated; (4) low-dose cerivastatin (0.2 mg/kg body weight per day) treated; and (5) medium-dose cerivastatin (0.4 mg/kg body weight per day) treated; and (6) high-dose cerivastatin (0.8 mg/kg body weight per day) treated. Groups 2-6 were treated for 23 weeks between the ages of 9 and 15 months and killed at the end of 23 weeks. The fourth lumbar vertebra was analyzed using peripheral quantitative computed tomography (pQCT). It is shown that age-matched controls had decreased cancellous bone mineral content (Cn. BMC) by 19% (p < 0.05) and cancellous bone mineral density Cn. BNID) by 22% (p < 0.01) when compared with baseline controls. All three doses of cerivastatin resulted in lower Cn. BMC and Cn. BNID when compared with age-matched controls, but this decrease was not statistically significant. In the PTH-treated group, Cn. BMC increased by 5% (p < 0.0001) and Cn. BMD increased by 37% (p < 0.0001) when compared with age-matched controls. In age-matched controls, cortical bone mineral content (Ct. BMQ and cortical bone mineral density (Ct. BMD) decreased slightly, but not significantly, when compared with baseline controls. Ct. BNID did not change significantly at any of the three doses in the cerivastatin-treated groups. In the PTH-treated group, Ct. BMC increased by 23% (p < 0.0001) when compared with age-matched controls. We confirmed that male SD rats lose bone with aging in the lumbar vertebra, and it is concluded that cerivastatin, at all doses administered, did not prevent this age-related bone loss. In contrast, PTH prevented age-related bone loss in the vertebra of male SD rats.
引用
收藏
页码:173 / 179
页数:7
相关论文
共 39 条
[1]  
[Anonymous], AGING SKELETON
[2]   Analysis of the effects of growth hormone, exercise and food restriction on cancellous bone in different bone sites in middle-aged female rats [J].
Banu, J ;
Orhii, PB ;
Okafor, MC ;
Wang, LP ;
Kalu, DN .
MECHANISMS OF AGEING AND DEVELOPMENT, 2001, 122 (08) :849-864
[3]  
Banu MJ, 2001, AGING-CLIN EXP RES, V13, P282
[4]   Cerivastatin: pharmacology of a novel synthetic and highly active HMG-CoA reductase inhibitor [J].
Bischoff, H ;
Angerbauer, R ;
Bender, J ;
Bischoff, E ;
Faggiotto, A ;
Petzinna, D ;
Pfitzner, J ;
Porter, MC ;
Schmidt, D ;
Thomas, G .
ATHEROSCLEROSIS, 1997, 135 (01) :119-130
[5]  
Bjarnason NH, 2000, J BONE MINER RES, V15, pS427
[6]   Hypertriglyceridemia: A review of clinical relevance and treatment options: Focus on cerivastatin [J].
Breuer, HWM .
CURRENT MEDICAL RESEARCH AND OPINION, 2001, 17 (01) :60-73
[7]  
Cauley JA, 2000, J BONE MINER RES, V15, pS155
[8]   Hypocholesterolemic effects of 3-hydroxy-3-methylglutaryl coenzyme a (HMG-CoA) reductase inhibitors in the guinea - Atorvastatin versus simvastatin [J].
Conde, K ;
Pineda, G ;
Newton, RS ;
Fernandez, ML .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (07) :1209-1219
[9]   INCIDENCE OF CLINICALLY DIAGNOSED VERTEBRAL FRACTURES - A POPULATION-BASED STUDY IN ROCHESTER, MINNESOTA, 1985-1989 [J].
COOPER, C ;
ATKINSON, EJ ;
OFALLON, WM ;
MELTON, LJ .
JOURNAL OF BONE AND MINERAL RESEARCH, 1992, 7 (02) :221-227
[10]   ANABOLIC ACTIONS OF PARATHYROID-HORMONE ON BONE [J].
DEMPSTER, DW ;
COSMAN, F ;
PARISIEN, M ;
SHEN, V ;
LINDSAY, R .
ENDOCRINE REVIEWS, 1993, 14 (06) :690-709